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By Corby G. Anderson

Today, with a stringent economic and environmental climate prevailing in the copper business, there is increased interest in evaluating new processing alternatives for production. Hydrometallurgical pressure oxidation of copper concentrates is one of the more viable approaches and several technological candidates have emerged. Of these, an overlooked but, ironically the first industrially proven methodology, utilized nitrogen species catalyzation in the oxidizing pressure leach system to produce copper via SX!EW. Given its many inherent process advantages, this may prove to be a feasible process alternative for the future. In this paper, the history of the system and its application to chalcopyrite concentrates will be outlined. In particular, a novel methodology for effective recovery of precious metals from chalcopyrite concentrates will be discussed. Finally, the perceived economics of this unique industrially proven process will be delineated.

Jan 1, 2000

By Sergei A. Degterov

A thermodynamic database for the slag, matte and liquid copper phases in the Cu-Ca-Fe-Pb-Zn-Si-O-S system has been developed for the ranges of compositions of importance to the production of copper. When used with the Gibbs energy minimization software and other databases of the F*A*C*T thermodynamic computing system, this database will permit the calculation of matte-slag-copper-gas phase equilibria that take place during copper smelting and converting. The calculations reproduce within experimental error limits all available experimental data on phase diagrams, activities of components, enthalpies of mixing, matte - alloy miscibility gap and tie-lines. The calculated solubilities of Cu in both S-free slag and slag equilibrated with matte are also in good agreement with experiment under all studied conditions, such as at SiO2 saturation, in equilibrium with Fe, Cu or Cu-Au alloys, at fixed oxygen or SO2 partial pressures and at different contents of Pb, Zn and CaO in the slag. Sulfide contents (sulfide capacities) of the slags are predicted within experimental error limits. The distribution of Pb and Zn among matte, slag, copper and gas has been calculated. The calculations are in good agreement with experimental data and predict the distributions under conditions which are difficult to study experimentally, such as at magnetite saturation or under various oxygen partial pressures and iron to silica ratios in the slag.

Jan 1, 1999

By Liwen Hu, Jianxun Song, Hongmin Zhu, Qiuyu Wang, Shuqiang Jiao

The subchloride titanium was prepared by sponge titanium and titanium tetrachloride in the CaCl2 at 1173 K. The species were detected are mainly titanium dichloride, and the average valent in the melt are 2.05. The accurate equilibrium constants were obtained for the reaction 3Ti2+ = 2Ti3++Ti after the accurate activities of titanium chloride were evaluated with emf method, and the observed deviations from ideal behavior are discussed.

Jan 1, 2015

By Robert Matusewicz

Ausmelt Technology has been applied to the recycling of spent pot liner (SPL) generated from primary alnminum production. The process is centered on the Ausmelt furnace, in which the SPL is converted under high temperature, oxidizing conditions to an HF containing gas stream and inert slag. fluorine is recovered from the SPL as HF gas and is concentrated and used to manufacture AIF) for recycle to the aluminum smelters. Approximately 87% of the fluorine can be recovered and converted to AIF), with the remainder being effectively tied up in the by product slag. Cost projections show that the recycling process will be competitive with other processes for SPL. The production and recycling of AIF) provides available credit that significantly offsets the operating cost of the facility. Ausmelt Technology for recycling of SPL is currently being marketed in North America by Ausmelt Technology Corporation in Denver, Colorado, and in the rest of the world by Ausmelt Limited of Dandenong, Australia.

Jan 1, 1996

By Pan Cao

The process of reduction roasting of nickel laterite with rotary hearth furnace combined with magnetic separation becomes a very potential way to prepare ferronickel alloy, especially for the low grade nickel laterite ore. In order to realize this new process, the effect of roasting temperature, time and additive on the reduction degree were investigated in the laboratory experimental. The results indicated that the recovery rate of Ni increased with the roasting temperature increasing to 1500°. Most of nickel and a spot of iron are selectively reduced with adding 25.19% SiO2, 6.42% coal, and roasting for 60min at 1500℃. Then conventional magnetic separation was carried out. The content of Ni and Fe are 7.50% and 59.08% in ferro-nickel nugget prepared by this method. And the recovery rate of Ni is 90.91%, which indicates that a high recovery of ferro-nickel from nickel laterite ore is achieved indeed.

Jan 1, 2014

By Ximena Diaz

Mercury is one of the most undesirable contaminants in gold bearing ores. During cyanidation mercury cyanide compounds accompany gold in all the extraction and recovery processes. Of course mercury in the carbon eluates creates environmental problems in subsequent refining steps. One possible process alternative for the separation of gold from mercury in such concentrated alkaline cyanide solutions is the selective solvent extraction of gold by undiluted Dibutyl Butyl Phosphonate (DBBP). In order to describe the behavior of mercury during extraction by DBBP, the results from a preliminary research program are presented. In this study, temperature and cyanide concentration have been found to be the most significant variables which influence the separation of gold from mercury by solvent extraction using DBBP. It was found, using plant eluate from a carbon strip, that excellent separation of gold from mercury can be obtained at 60' C with 98% gold recovery and complete mercury rejection in a single stage of extraction. The influence of pH is also discussed in terms of the extraction chemistry. These results complement previous research which described the DBBP solvation extraction of an aurocyanide ion pair. In addition, these results extend our understanding of the alkyl phosphorous ester extraction systems by illustrating that neutral ionic species such as Hg(cN)02sq, can be extracted at low cyanide concentrations, a phenomenon which had not been observed previously for other cyanoanions.

Jan 1, 1993

By Huaming Yang

The vanadium-doped SnO2 nanoparticle was synthesized by the co-precipitation reaction and subsequent calcination from the vanadium(III) chloride and tin(IV) chloride. The crystal size, pore size distribution, micrograph and properties of the nanocrystalline powders were examined by differential thermal analysis (DTA), thermogravimetric analysis (TGA), X-ray diffraction (XRD), desorption isotherm (Barrett-Joyner-Halenda method) and transmission electron microscopy(TEM). Thermal treatment of the precipitate powder at 600°C led to the formation of V -SnO2 nanoparticle of -10mm in crystal size. Most of the pores in the nanoparticle are about 5~15nm in diameter. Effect of doped vanadium on the crystal size of the nanopartic1e was discussed.

Jan 1, 2003

By Zhangm Mingming

Three samples received from the EAF shop were characterized by chemical, X-ray diffraction (XRD), optical microscopy (OM) and scanning electron microscopy (SEM) methods. The objective of this characterization work was to investigate the occurrence of nickel, copper, zinc, sulfur and phosphorus and to identify their origin and associations with iron minerals in the concentrate samples from the mines. The samples were identified as MINERAL, PELLET, and HRD. The latter is the DRI product. All three samples were received as fine powders. The results indicate that, in the mineral sample, magnetite is the major iron oxide mineral with hematite as a second phase based on the OM and XRD studies. Pyrite [FeS2], chalcopyrite [CuFeS2] and bravoite [(Fe,Ni)S2] are the major sulfide minerals. Trace amounts of apatite [Ca5(PO4)3(F,Cl,OH)], wardite [Na4CaAli2(PO4)8(OH)8 6H2O], giniite [Fe;(PO4)4(OH)3 2H2O] and vivianite [Fe3(PO4)2 8H2O] were identified by SEM and XRD. Microscopic studies also indicated that most of the sulfide grains in the mineral sample are present either as liberated fine particles (about 10 microns) or as inclusions within the magnetite and hematite grains. XRD studies revealed magnetite as the major mineral with subordinate amounts of hematite and pyrite confirming the microscopic findings. Copper, nickel, and zinc are mainly present as chalcopyrite, bravoite, and franklinite [(Zn,Mn,Fe)(Fe,Mn)2O4] in trace amounts in the mineral samples, respectively. Impurities carry over to the pellet and HRD samples. Chemical analyses of the three iron-bearing samples indicate that sulfur and phosphorus in the pellet sample exceeded the specification. Since liberated pyrite and chalcopyrite particles were observed in both the mineral and pellet samples, magnetic and flotation processing routes should be effective for sulfide removal but at the cost of iron losses. The high phosphorus content of all three samples indicates that there are phosphates which are difficult to remove by the current concentrating processes (magnetic separation and flotation).

Jan 1, 2012

By E. Salinas-Rodriguez, J. Hernández-Ávila, E. O. Ávila-Dávila, A. Romero-Serrano, M. Perez-Labra, G. Juárez-López

"Single phase rubidium jarosite was synthesized by precipitation from aqueous solution. X-ray diffraction and SEM-EDS analyses showed that the synthetic rubidium jarosite formed in subspherical particles with an average particle size of about 35 µm. The chemical analysis showed an approximate composition of Rbo9432Fe3(SO4)2 1245(OH)6. The decomposition behaviour of the jarosite in terms of solution pH was thermodynamically modeled using FACTSage by constructing the potential-pH diagram at 298.15 K. The E-pH diagram showed that the decomposition of jarosite leads to goethite (FeOOH) together with Rb+ and SO42- ions. The experimental decomposition of the Rb-jarosite was carried out in alkaline solutions with five different Ca(OH)2 concentrations. The decomposition process showed an ""induction period"" followed y a progressive conversion period where the Rb+ and SO42- ions formed in the aqueous solution. In contrast, calcium was incorporated in the solid residue and iron was transformed into amorphous ferrihydrite. The kinetic analysis showed that this process can be represented by the unreacted-core chemically controlled model. The reaction order with respect to Ca(OH)2 is 0.4342 and the calculated activation energy is 98.70 kJ mol-1. IntroductionJarosite type compounds are hydrous sulfate minerals containing alkalis and ferric ions, MFe3(SO4)2(OH)6, where M can be H3O+· Na+, K+, Rb+, Ag+, NH4 +, Tl+, ½ Pb2+ or ½ Hg2+. Jarosite-type compounds were formed by the natural ""in situ"" oxidation of pyritic ores leading to the replacement of the original iron sulfides and iron oxides (Dutrizac and Kaiman) [1]. The great interest in jarosites is due to its ability to eliminate or diminish the iron concentration of the acid leach solutions produced in the hydrometallurgical zinc process, with relatively low losses of divalent metals such as Zn2+, Cd2+, Cu2+ or Co . However, the losses of the metal values demand a careful study of the conditions under which the jarosite compounds are formed together with their chemical properties."

Jan 1, 2012

By Ruth Marlene Campomanes Santana, Michel Tieccher, Marcondes Mafacioli Pacheco, Juliano Urach

"IntroductionThe gaseous emissions of fuel burning by mobile sources are responsible for incidence and increase of many lung and cardiovascular diseases (Braga et al., 2007). These implications can watch in morbity as much as mortality, even when the levels of pollution are considerate restrained or lower. (Leite et al., 2002).Sample of mobile sources exhausts contain not only particles directly shaped by burning, but also secondary particles that results of reaction between other compounds (Burtscher, 2004).One of the principal pollutants produced by combustion process with major toxicity and raiser of adverse effects to health is the particulate material. In its constitution there are fine and ultrafine particles that can to extend deep portion of breath system, break epithelial barrier and reach the interstitial of lungs and then, to unleash inflammatory process (Arbex, 2004).The Particulate Material is employed to define a mixture of solid particles and liquid drops suspense in atmosphere. Queiroz et al. (2007) declare that this material can be divided in two types separated by size interval that together, represent the major class of disperse particles: the fine particles type of 2,5 µm de (breath particulate) and the type of earthliness particles, major than 2,5 µm to 10 µm (inhale particle). The difference of size between the particles influences on the physics and chemistry properties. They affirm that exist correlation between size of particle and heavy metals; how many lower was the dimension of particulate materials, major is the concentration of heavy metals.The inhale particulate (MP10) that is object of present study can exhibit in your composition sulfates, nitrates, amoniacal, marine salt (NaCl), soil elements (Al, Ca, Fe, Si, Ti), metals (Cd, Cr, Cu, Ni, Pb, V, Zn) and water (Queiroz et al., 2007).Recent studies have exhibit strong relation between daily levels of particulate material inhale (MP10) with diameter until 10 µm and others pollutants and one infinity of effects to health that go since total mortality of population, sicken for specific causes until congenital bad formation or even difficult win weight by the fern during gestation (Gouveia et al., 2006)."

Jan 1, 2008

By Susumu Nagae, Hajime Ikeda

Recently, a number of mine development projects have been setback by social, economic and, environmental circumstances that had not been seen before. Many of these problems do not always originate from direct mine pollution. Typical examples of these are· conflicts between the exploration company and the local residents, sudden objections just before the development is to begin, and unexpected tightening of environmental regulations. The common background to these problems is expanding global environmental awareness. This includes complex factors ·such as the expansion of exploration to remote regions, the brisk activities of environmental NGOs, the increase of international environmental laws and, governmental policy changes. Today, the range of issues concerning mine development is widening significantly. The participation of local residents arid NGOs in the development planning, together with the company and government, has become essential for smoothly carrying out mine projects and making them more beneficial for stakeholders. Introduction The common image of the environmental problem with respect to mining is direct mine pollution, such as the collapse of tailings dams, pollution from refineries, and acid mine drainage. All over the world, the mining industry has made large investments in capital and technology to solve and prevent mine pollution, and these efforts have been making steady achievements. However in recent years, new cypes of environmental problems which are not originating directly from mine pollution are emerging frequently. Most of the problems are concentrated at the exploration stage to early stage of development, which have less impact on the environment. In the worst case, mining project may be forced to cancel and could cause serious damage to the industry because they could not collect their investment. I would like to take a general view of the examples of new types of trouble, their characters, background, and strategies against these problems.

Jan 1, 2000

By James O'Brien, Lyman Frost, S. Elangovan, J. Stephen Herring, Joseph Hartvigsen, Carl Stoots, Anthony Nickens

"Carbon dioxide recovered from concentrated sources, such as metallurgical reduction furnaces, cement kilns and fossil power plants can provide a valuable feedstock for a synthetic fuels industry based on energy from nuclear, solar, wind and hydropower sources. High temperature co-electrolysis of CO2 and steam to produce synthesis gas has been demonstrated using reversible solid oxide fuel cell technology. Where a source of high temperature process heat is available, such as from an advanced high temperature nuclear reactor or solar dish concentrator, the endothermic electrolysis reactions can utilize both thermal and electrical inputs in such a way that the conversion efficiency within the cell is 100%. Synthesis gas produced in a coelectrolysis cell has been further reacted over a catalyst to produce conventional hydrocarbon fuels. Widespread implementation of synfuel production from CO2 will enable a much larger reliance on intermittent renewable energy than can be accommodated by conventional electric demand profiles.IntroductionFor the past several years, Ceramatec, Inc and the Idaho National Laboratory (INL), have been studying the feasibility of high temperature solid oxide electrolysis for large-scale, nuclearpowered hydrogen production under the U.S. DOE’s nuclear hydrogen initiative (NHI) as an alternative to the thermochemical process. Parallel to this effort, the INL and Ceramatec have been researching high temperature co-electrolysis of mixtures of steam and CO2 to produce syngas:"

Jan 1, 2008

By S. Malinov, J. J. McKeown, W. Sha, S. McShane

"A model is developed for prediction of fatigue stress life S-N diagrams for Ti-6Al-4V alloy at different conditions, using Artificial Neural Network (ANN). Different factors which have influence on the S-N diagram are involved as input parameters of the NN, namely microstructure, environment, texture, test/work temperature, surface treatment and stress amplitude. As the output the S-N fatigue diagram is simulated and plotted.The model is based on standard multilayer feedforward neural network. The NN is trained with a comprehensive data set collected from the literature, using Levenberg-Marquardt training algorithm in combination with Bayesian regularisation. A very good performance of the trained Neural Network is achieved. Good correspondence between ANN"" prediction and experimental S-N diagrams is observed. Using the model S-N diagrams for different conditions are predicted and analysed. Graphical User Interface is developed for use of the model. We believe that the model will be important for practical applications in solving various problems on fatigue behaviour of the titanium alloy.IntroductionTitanium and its alloys have an increasing range of applications due to their very good combination of mechanical properties, corrosion and erosion resistance. They are currently finding widespread applications in many industries due to their desirable and versatile properties. Most important among the alloys is Ti-6AI-4Y. Jet aircraft manufacturers are the principal 'consumers of Ti-6Al-4V and it is often specified for critical parts, the failure of which could result in the loss of an entire system. A generic class of Ti-6AI-4V has been developed over the past years and it has become the best understood of all the titanium alloys. The advantages of titanium alloys include: (i) low densities, giving very attractive strength to weight ratios allowing lighter and stronger structures; (ii) superior corrosion and erosion resistance in many environments; (iii) high temperature capability. Although the titanium materials are still considered as expensive materials, for many applications the cost of titanium alloys can be justified on the basis of their desirable properties."

Jan 1, 2001

By Shubin Wang

Copper(II) and nickel(II) are often recovered from ammoniacal alkaline solutions by solvent extraction using hydroxyoxime extractants: both copper(II) and nickel(II) are extracted from ammoniacal alkaline solutions and, from the loaded organic phase, nickel(II) is selectively stripped with a dilute acid followed by copper(II) stripping with an acid of higher concentration. Since a small portion of ammonia is co-extracted with copper and nickel, the extracted ammonia should be scrubbed using a dilute acid before metal stripping. In the present study, a mechanistic model has been developed in order to support design and control of this process. The equilibrium distribution ratios of copper(II), nickel(II), and ammonia at 298 K using LIX® 84-I (active component, 2-hydroxy-5-nonylacetophenone oxime) as the extractant are successfully correlated by considering the relevant equilibria. Based on these results, quantitative prediction of equilibrium distribution ratios in the process has been made possible, and suitable conditions for the efficient separation of copper(II) and nickel(II) are discussed.

By Mingming Zhang

"Three samples received from the EAF shop have been characterized by chemical, X-ray diffraction (XRD), optical microscopy (OM) and scanning electron microscopy (SEM) methods. The objective of this characterization work is to investigate the occurrence of nickel, copper, zinc, sulfur and phosphorus in these samples and identity their origin and associations with iron minerals in the concentrate samples that are from mines.The samples were identified as Mineral, Pellet, and HRD. The latter is the DR! product. All three samples were received as fine powders. The results indicate that, in the mineral sample, magnetite is the major iron oxide mineral with hematite as a second phase based on the OM and XRD studies. Pyrite [FeS2], chalcopyrite [CuFeS2] and bravoite [(Fe,Ni)S2] are major sulfide minerals. Trace amounts of apatite [Ca5(P04)3(F,Cl,OH)], wardite [Na4CaA112(P04)8(OH)8 6H20], giniite [Fe5(P04)4(OH)3 2H20] and vivianite [Fe3(p04)2 8H20] were identified by SEM and XRD. Microscopic studies also indicated that most of the sulfide grains in the mineral sample are present either as liberated fine particles (about 10 microns) or as inclusions within the magnetite and hematite grains. XRD studies revealed magnetite as the major mineral with subordinate amounts of hematite and pyrite confirming the microscopic findings. Copper, nickel, and zinc are mainly present as chalcopyrite, bravoite, and franklinite [(Zn,Mn,Fe)(Fe,Mn)204] in trace amount in the mineral samples, respectively. Impurities carry over to the Pellet and HRD samples.Chemical analyses of the three iron-bearing samples indicate that sulfur and phosphorus in the Pellet sample exceeded the specification. Since liberated pyrite and chalcopyrite particles were observed both in mineral and pellet samples, magnetic and flotation processing routes for this ore should be effective for sulfide removal but at the cost of iron losses. The high phosphorus content of all three samples indicates that there are phosphates which are difficult to remove by the current concentrating process (magnetic separation and flotation)"

Jan 1, 2012

By Nicola Baldo, Marco Pasetto

"The paper discusses the results of a laboratory study, aimed to evaluate the suitability of the bottom ash from Municipal Solid Waste Incineration (MSWI), obtained from different Italian plants, to be recycled in the lithic skeleton of bituminous mixtures, for base layers of road and airport pavements. The research involved a preliminary study of the physical and geotechnical properties of the bottom ash by itself; it was followed by a mechanical characterization of the bituminous concretes. The traditional Marshall methodology was used to identify the optimum bitumen content; the mixtures were also mechanically checked by means of the stiffness modulus test, repeated load axial test and fatigue test. Because the requisites for acceptance in the Italian Specifications and Standards have been satisfied and given the positive mechanical performances, it has been verified that the MSWI bottom ash can be used as substitution of the lithic materials in the road bases, also with very high contents (up to 81% on the weight of the aggregate). Introduction The incineration of Municipal Solid Wastes (MSWs) provides for by-products which can be mainly classified as bottom ash and fly ash. The first one, corresponding to the 25% on the weight of the wastes to be incinerated, so resulting the principal product of the process, is mainly composed by Silica (Si), Iron (Fe), Calcium (Ca), Aluminium (Al), Sodium (Na) and Potassium (K) oxides, so presenting a composition similar to that of different natural materials. Its metallic fraction can be recovered; the remaining part is usually stocked in dumping or, less frequently, recycled. Bottom ash can be re-utilised in the construction of new infrastructures, especially in bitumen bounded mixtures, because of the inert properties of the binder which covers the grains with a subtle film, that prevents the release of heavy metals. The paper describes a study aimed to design new bituminous mixes for flexible road and airport pavements, realised with the highest content of 4 types of bottom ashes, deriving from different MSWI plants of the Northern Italy. The ashes will be named as BA1, BA2, BA3, BA4 respectively (the origin cannot be specified)."

Jan 1, 2008

By Abhishek Lahiri, Animesh Jha

"A new technique for the selective separation of rare earths and impurities from lower grade titaniferous ores has been developed which will reduce the overall reduction in the energy costs, and therefore the CO2 generation by at least an order of magnitude during the chlorination and waste handling stages of TiO2 to TiCl4 reaction. The process includes roasting the ilmenite ore with alkali followed by water washing step, which removes nearly 80% of oxides of lanthanide and actinide elements present in lower grades of titaniferous minerals. In the context of preferential separation of rare- 3+ + earth and actinide oxides, we have examined the roles of Al and K ions on the lattice structures of ilmenite and complex titanate as the product layer forms during the roasting in air in the presence of potash. The composition of the mixtures of oxides derived from the separation process shows that the mixture of rare-earth oxides m ay be a high-value co-product of the overall beneficiation process.IntroductionWorldwide the production of synthetic rutile is carried out either by the sulphate or the slag-making followed by fluidised bed chlorination of TiO2 enriched slag granules. The chlorinated gas is then re-oxidized to make white pigment grade TiO2. The waste generated by the sulphate process is predominantly iron sulphate, which has limited use in the water treatment plant. The remaining wastes from the sulphate process undergo further treatment using filtration followed by evaporation and thermal decomposition after which it is disposed into deep sea. On the other hand the chloride waste is extremely hazardous and requires special case by neutralisation, followed by impoundment in a managed pond, where it is monitored for long-term for potential contamination to the soil and ground water. Rare-earth and prelanthanide wastes often end up in the pond where they are diluted and irretrievably lost for further use or recycle. Certain parts of the world the chloride process wastes are pumped via deep boreholes into porous geological strata. The present techniques of disposal are not only expensive but also pose continued threat groundwater and soil and marine life in case of sulphate waste [1, 2]."

Jan 1, 2009

By Huaming Yang

The vanadium-doped SnO2 nanoparticle was synthesized by the co-precipitation reaction and subsequent calcination from the vanadium(III) chloride and tin(IV) chloride. The crystal size, pore size distribution, micrograph and properties of the nanocrystalline powders were examined by differential thermal analysis (DTA). thermogravimetric analysis (TGA). X-ray diffraction (XRD), desorption isotherm (Barrett-Joyner-Halenda method) and transmission electron microscopy (TEM). Thermal treatment of the precipitate powder at 600'C led to the formation of crystal0nmincrystal size. Most of the pores in the narmparticle are about 5~15nm in diameter. Effect of doped vanadium on the crystal size of the nanoparticle was discussed.

Jan 1, 2003

By W. Riekehof

The paper explains required practice and equipment for capturing airborne fumes and particulates in hot-dip zinc galvanizing plants. An economic and technical comparison of enclosure and tank rim suction options is presented. The paper also compares the performance of various filter media in filtering fumes, to determine the effect of changes in flux as well as changes in filter finishlcoating methods. This includes a recommendation for how to achieve the best result with respect to pressure loss and cleaning behavior of the filter.

Jan 1, 1992

By Sridhar Komarneni

"Microwave-hydrothermal processing is a novel technique which combines the conventional hydrothermal processing with microwave field and we previously showed for the first time, that ceramic powders can be rapidly produced by this technique. This review paper deals with the synthesis of unary oxides such as Fe203, Ti02, Zr02, etc., binary oxides such as BaTiO3, SrTiO 3, PbTiO 3, SrZrO 3, KNbO3, etc., and ternary oxides such as NaTi2 (PO4)3 and pyrochlore phases of Pb(Mg1/3Nb2/3)O3, Pb(Zn1/3Nb2/3)O3 etc. and metal powders such as Cu, Ni, etc. below 195°C. This method can be adopted to the synthesis of a large variety of powders by the appropriate control of pH, Eh, temperature/pressure and concentration of chemical species. The main advantages of this method compared to conventional hydrothermal processing are (a) it increases the kinetics of reaction by one to two orders of magnitude, and (b) it can lead to novel phases especially those with layered structures.IntroductionConventional hydrothermal processing is a well-established synthesis technique which has been extensively used in the preparation of fine ceramic powders [1-5], large single crystals [6-8] and massive cement blocks [9]. Technologically important ceramic powders such as BaTiO 3, Al203 etc. made by the hydrothermal process are now commercially available. Although there are numerous methods for materials synthesis, hydrothermal method is truly a low temperature and environmentally benign process. For example, ZrSi04 (Zircon) which is extensively used in ceramic industry can be prepared hydrothermally at 150·C [10] compared to sol-gel or solid-state method [11,12] which require a temperature of about 1000·C. The hydrothermal method is environmentally benign because hydrothermal reactions are carried out in closed systems at low temperatures and the contents can be recovered and recycled after cooling to the ambient conditions. One of the disadvantages with any low temperature processing method is slow kinetics. For this reason we have combined the hydrothermal method with microwaves to enhance kinetics and we named this method as ""Microwave-hydrothermal"" processing [13- 16]. Although the combination of microwave and hydrothermal techniques has been used in the past few years to dissolve all kinds of inorganic (e.g. alumino silicate rocks) and organic materials rapidly for chemical analysis, we were the first to show its potential value for the synthesis of various ceramic powders [13-16]. In this paper, I show that this novel method is applicable to the synthesis of all unary, binary and multinary oxides by the appropriate control of pH, Eh, temperature, pressure and concentration of chemical species. In addition, this method is also found to be useful for the preparation of metal powders."

Jan 1, 1994